The effect of trichlormethiazide in autosomal dominant polycystic kidney disease patients receiving tolvaptan: a randomized crossover controlled trial
Abstract The vasopressin V2 receptor antagonist tolvaptan delays the progression of autosomal dominant polycystic kidney disease (ADPKD). However, some patients discontinue tolvaptan because of severe adverse aquaretic events. This open-label, randomized, controlled, counterbalanced, crossover trial...
Guardado en:
Autores principales: | Kiyotaka Uchiyama, Chigusa Kitayama, Akane Yanai, Yoshitaka Ishibashi |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/edc0d792befa40818f671fc0aec063c5 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Treatment persistence to tolvaptan in patients with autosomal dominant polycystic kidney disease: a secondary use of data analysis of patients in the IMADJIN® dataset
por: Mark Thomas, et al.
Publicado: (2021) -
Echocardiographic Findings and Genotypes in Autosomal Dominant Polycystic Kidney Disease
por: Ryohei Miyamoto, et al.
Publicado: (2021) -
Identification of pathological transcription in autosomal dominant polycystic kidney disease epithelia
por: Sebastian Friedrich, et al.
Publicado: (2021) -
Metabolic profiling in children and young adults with autosomal dominant polycystic kidney disease
por: Madhurima M. Baliga, et al.
Publicado: (2021) -
Cinacalcet may suppress kidney enlargement in hemodialysis patients with autosomal dominant polycystic kidney disease
por: Shinya Nakatani, et al.
Publicado: (2021)